93560-49-7

Usage

Uses

Used in Flavor and Fragrance Industry:
2-(2-FURANOYL)PYRIDINE is utilized as a flavoring agent in the flavor and fragrance industry, owing to its sweet, caramel-like taste and aroma. It is commonly found in foods and beverages as a natural flavoring, enhancing the sensory experience for consumers.
Used in Perfume Manufacturing:
In addition to its use in food and beverages, 2-(2-FURANOYL)PYRIDINE is also employed in the production of perfumes and other scented products. Its unique aroma contributes to the creation of various fragrances, making it a valuable component in the perfumery sector.

Upstream product

• 93560-48-6 C-Furan-2-yl-C-pyridin-2-yl-methyleneamine 
• 110-00-9 furan 
• 100-70-9 2-Cyanopyridine 
• 109-04-6 2-bromo-pyridine 
• 617-90-3 2-furancarbonitrile 
• 106584-05-8 2-(furan-2-ylmethyl)pyridine 
• 109-06-8 α-picoline 
• 941279-81-8 2,4-dimethyl-3-(pyridin-2-ylmethyl)pentan-3-ol 

Downstream Products

• 95898-98-9 2-furyl-2-pyridinylmethanamine 
• 959083-28-4 furan-2-yl(pyridin-2-yl)methanol 

Relevant academic research and scientific papers

Efficient Selenium-Catalyzed Selective C(sp3)?H Oxidation of Benzylpyridines with Molecular Oxygen

An efficient selenium-catalyzed direct oxidation of benzylpyridines in aqueous DMSO has been successfully developed by using molecular oxygen as the oxidant. A variety of benzoylpyridines with broad functional group tolerance were obtained in modest to excellent yields and with exclusive chemoselectivity. (Figure presented.).

Synthesis of 2-heteroaryl-3-hydroxypyridines by ring expansion reactions of 2-acylfurans with ammonia

A straightforward and versatile synthesis of 2-heteroaryl-3-hydroxypyridine derivatives is described by the one-step reaction of 2-acylfurans with ammonia at 150°C.

Synthesis and Properties of 2,2'-Bipyridin-3-ols and -3,3'-diols

The synthesis of the 2-furyl ketones 5-7 and 13 and their reaction with ammonium acetate in boiling acetic acid to 3-substituted 2,2'-bipyridines and to 2-(2-pyrimidinyl)-3-pyridinol (14) via a ring-transformation reaction are described.Strong intramolecular hydrogen bonds are responsible for their physical and chemical properties.